rs61751364, MECP2

N. diseases: 4
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Rett Syndrome
CUI: C0035372
Disease: Rett Syndrome
54 0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 0.770 1.000 7 2005 2016
Epilepsy
CUI: C0014544
Disease: Epilepsy
250 0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 0.010 1.000 1 2010 2010
Pain
CUI: C0030193
Disease: Pain
182 0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 0.010 1.000 1 2010 2010
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
15 0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 0.010 1.000 1 2010 2010